Results 41 to 50 of about 19,821 (199)

Examination of Dietary Patterns and FODMAPs Intake in Patients with Irritable Bowel Syndrome [PDF]

open access: yes, 2020
Background: There is growing evidence that supports the efficacy of a diet low in fermentable oligosaccharides, disaccharides, monosaccharides, and polyols (FODMAPs) for symptom management in irritable bowel syndrome (IBS).
Pei, Xuechen
core  

A single supplement of a standardised bilberry (Vaccinium myrtillus L.) extract (36 % wet weight anthocyanins) modifies glycaemic response in individuals with type 2 diabetes controlled by diet and lifestyle [PDF]

open access: yes, 2013
Peer reviewedPublisher ...
Bestwick, Charles   +6 more
core   +1 more source

Insuficiencia hepática aguda asociada a enfermedades metabólicas hereditarias en ninos pequenos [PDF]

open access: yes, 2017
INTRODUCTION: Pediatric acute liver failure (ALF) due to inherited metabolic diseases (IMD) is a rare life-threatening condition with a poor prognosis. Early intervention may be lifesaving.
Dias-Costa, F   +6 more
core   +1 more source

Fructosuria and recurrent hypoglycemia in a patient with a novel c.1693T>A variant in the 3′ untranslated region of the aldolase B gene

open access: yesSAGE Open Medical Case Reports, 2019
Hereditary fructose intolerance, caused by mutations in the ALDOB gene, is an unusual cause of hypoglycemia. ALDOB encodes the enzyme aldolase B, responsible for the hydrolysis of fructose 1-phosphate in the liver.
Martha Catalina Morales-Alvarez   +4 more
doaj   +1 more source

Fructose: role in the formation of intestinal symptoms

open access: yesGastroenterologìa, 2022
Fructose is a simple sugar that is present in fruit and honey, but is also a major component in the two most commonly used sweeteners, sucrose (table sugar), and high fructose corn syrup (HFCS).
N.N. Silivontchik
doaj   +1 more source

Inborn errors of metabolism: a clinical overview [PDF]

open access: yes, 1999
CONTEXT: Inborn errors of metabolism cause hereditary metabolic diseases (HMD) and classically they result from the lack of activity of one or more specific enzymes or defects in the transportation of proteins.
Martins, Ana Maria
core   +4 more sources

Adult hereditary fructose intolerance

open access: yesWorld Journal of Gastroenterology, 2009
Hereditary fructose intolerance (HFI) is an under-recognized, preventable life-threatening condition. It is an autosomal recessive disorder with subnormal activity of aldolase B in the liver, kidney and small bowel. Symptoms are present only after the ingestion of fructose, which leads to brisk hypoglycemia, and an individual with continued ingestion ...
Mohamed Ismail, Yasawy   +3 more
openaire   +2 more sources

The unexpected truth about dates and hypoglycemia

open access: yesJournal of Family and Community Medicine, 2016
Background: Dates are a concentrated source of essential nutrients, vitamins, minerals, and carbohydrates (CHOs), which are necessary for the maintenance of optimum health. Most of the CHOs in dates come from sugars including glucose and fructose.
Mohammed I Yasawy
doaj   +1 more source

Gender Differences in Bile Acids and Microbiota in Relationship with Gender Dissimilarity in Steatosis Induced by Diet and FXR Inactivation. [PDF]

open access: yes, 2017
This study aims to uncover how specific bacteria and bile acids (BAs) contribute to steatosis induced by diet and farnesoid X receptor (FXR) deficiency in both genders.
French, Samuel W   +8 more
core   +1 more source

DIAGNOSIS DIFFICULTIES IN SEVERE AND CHRONIC HEPATOPATHY WITH EARLY ONSET. CASE REPORT [PDF]

open access: yesRomanian Journal of Pediatrics, 2014
Authors emphasize diagnosis and treatment diffi culties in a patient with severe and chronic idiopathic hepatopathy. Authors present a 5 year-old male frequently admitted for severe acute liver failure episodes with severe gastrointestinal bleedings that
Sorin Ioan Iurian   +2 more
doaj   +1 more source

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